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Product Description
Valacyclovir is a prodrug of Acyclovir (Cat.No. 2200-50, 250) with inhibitory activity against herpes simplex virus types 1 (HSV-1), 2 (HSV-2), varicella-zoster virus (VZV), Epstein-Barr virus (EBV), and cytomegalovirus (CMV). Valacyclovir is phosphorylated by viral thymidine kinase to acyclovir triphosphate (the active metabolite) which then inhibits herpes viral DNA replication by competitive inhibition of viral DNA polymerase, and by incorporation into and termination of the growing viral DNA chain.
Valacyclovir is a prodrug of Acyclovir (Cat.No. 2200-50, 250) with inhibitory activity against herpes simplex virus types 1 (HSV-1), 2 (HSV-2), varicella-zoster virus (VZV), Epstein-Barr virus (EBV), and cytomegalovirus (CMV).
Biovision | 2201 | Valacyclovir Hydrochloride Hydrate DataSheet
Alternate Name/Synonyms: L-Valine 2-(2-Amino-1,6-dihydro-6-oxo-9H-purin-9-ylmethoxy)ethyl Ester Hydrochloride hydrate; valaciclovir
Appearance: White solid
Formulation: N/A
CAS Number: 124832-27-5
Structure Available?: Yes
Peptide sequence: N/A
Salt Form: No
Molecular Formula: C₁₃H₂₀N₆O₄·HCl·xH2O
Molecular Weight: 360.80 (anhydrous basis)
Cell-Permeable?: Yes
Purity: ≥97% by HPLC
Solubilities: H₂O (>20 mg/ml)
Handling: Protect from air and moisture
Country of Origin: USA
Tag Line: An antiviral agent
MDL Number: MFCD01861507
PubChem CID: 60772
SMILES: CC(C)C(C(=O)OCCOCN1C=NC2=C1NC(=NC2=O)N)N.Cl
InChi: InChI=1S/C13H20N6O4.ClH/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20;/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20);1H/t8-;/m0./s1
InChi Key: ZCDDBUOENGJMLV-QRPNPIFTSA-N
